Point mutations in the abl SH2 domain coordinately impair phosphotyrosine binding in vitro and transforming activity in vivo - PubMed (original) (raw)
Point mutations in the abl SH2 domain coordinately impair phosphotyrosine binding in vitro and transforming activity in vivo
B J Mayer et al. Mol Cell Biol. 1992 Feb.
Abstract
We have constructed a series of point mutations in the highly conserved FLVRES motif of the src homology 2 (SH2) domain of the abl tyrosine kinase. Mutant SH2 domains were expressed in bacteria, and their ability to bind to tyrosine-phosphorylated proteins was examined in vitro. Three mutants were greatly reduced in their ability to bind both phosphotyrosine itself and tyrosine-phosphorylated cellular proteins. All of the mutants that retained activity bound to the same set of tyrosine-phosphorylated proteins as did the wild type, suggesting that binding specificity was unaffected. These results implicate the FLVRES motif in direct binding to phosphotyrosine. When the mutant SH2 domains were inserted into an activated abl kinase and expressed in murine fibroblasts, decreased in vitro phosphotyrosine binding correlated with decreased transforming ability. This finding implies that SH2-phosphotyrosine interactions are involved in transmission of positive growth signals by the nonreceptor tyrosine kinases, most likely via the assembly of multiprotein complexes with other tyrosine-phosphorylated proteins.
Similar articles
- Direct analysis of the binding of the abl Src homology 2 domain to the activated epidermal growth factor receptor.
Zhu G, Decker SJ, Mayer BJ, Saltiel AR. Zhu G, et al. J Biol Chem. 1993 Jan 25;268(3):1775-9. J Biol Chem. 1993. PMID: 7678409 - Reduced phosphotyrosine binding by the v-Src SH2 domain is compatible with wild-type transformation.
Tian M, Martin GS. Tian M, et al. Oncogene. 1996 Feb 15;12(4):727-34. Oncogene. 1996. PMID: 8632894 - A limited set of SH2 domains binds BCR through a high-affinity phosphotyrosine-independent interaction.
Muller AJ, Pendergast AM, Havlik MH, Puil L, Pawson T, Witte ON. Muller AJ, et al. Mol Cell Biol. 1992 Nov;12(11):5087-93. doi: 10.1128/mcb.12.11.5087-5093.1992. Mol Cell Biol. 1992. PMID: 1383690 Free PMC article. - The carboxyl terminus of v-Abl protein can augment SH2 domain function.
Warren D, Heilpern AJ, Berg K, Rosenberg N. Warren D, et al. J Virol. 2000 May;74(10):4495-504. doi: 10.1128/jvi.74.10.4495-4504.2000. J Virol. 2000. PMID: 10775585 Free PMC article.
Cited by
- A side-by-side comparison of variant function measurements using deep mutational scanning and base editing.
Sokirniy I, Inam H, Tomaszkiewicz M, Reynolds J, McCandlish D, Pritchard J. Sokirniy I, et al. bioRxiv [Preprint]. 2024 Sep 26:2024.06.30.601444. doi: 10.1101/2024.06.30.601444. bioRxiv. 2024. PMID: 39005366 Free PMC article. Preprint. - Cell-permeable PI3 kinase competitive peptide inhibits KIT mutant mediated tumorigenesis of gastrointestinal stromal tumor (GIST).
Jiang Z, Guo Y, Shi J, Zhang S, Zhang L, Wang Y, Li G, Bai R, Zhao H, Sun J. Jiang Z, et al. Mol Biol Rep. 2024 Jan 11;51(1):98. doi: 10.1007/s11033-023-09120-x. Mol Biol Rep. 2024. PMID: 38206538 - Stimulation of the catalytic activity of the tyrosine kinase Btk by the adaptor protein Grb2.
Nocka LM, Eisen TJ, Iavarone AT, Groves JT, Kuriyan J. Nocka LM, et al. Elife. 2023 Apr 26;12:e82676. doi: 10.7554/eLife.82676. Elife. 2023. PMID: 37159508 Free PMC article. - The SH2 domain and kinase activity of JAK2 target JAK2 to centrosome and regulate cell growth and centrosome amplification.
Shahi A, Kahle J, Hopkins C, Diakonova M. Shahi A, et al. PLoS One. 2022 Jan 28;17(1):e0261098. doi: 10.1371/journal.pone.0261098. eCollection 2022. PLoS One. 2022. PMID: 35089929 Free PMC article. - SH2 Domain Binding: Diverse FLVRs of Partnership.
Jaber Chehayeb R, Boggon TJ. Jaber Chehayeb R, et al. Front Endocrinol (Lausanne). 2020 Sep 18;11:575220. doi: 10.3389/fendo.2020.575220. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 33042028 Free PMC article. Review.
References
- Cell. 1991 Jan 25;64(2):281-302 - PubMed
- Science. 1990 Jun 22;248(4962):1537-9 - PubMed
- J Virol. 1990 Aug;64(8):3581-9 - PubMed
- Proc Natl Acad Sci U S A. 1990 Nov;87(21):8592-6 - PubMed
- Proc Natl Acad Sci U S A. 1990 Nov;87(21):8622-6 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous